A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021851



Internal ID19111069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:145727123..145807997hg38UCSC Ensembl
Innerchr5:145106686..145187560hg19UCSC Ensembl
Innerchr5:145086879..145167753hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3880875
hg1980875
hg1880875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648158
Samples
Known GenesPRELID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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